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胰高血糖素瘤综合征伴非典型坏死性游走性红斑。

Glucagonoma syndrome with atypical necrolytic migratory erythema.

机构信息

Department of Dermatology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

Department of Dermatology, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.

出版信息

Indian J Dermatol Venereol Leprol. 2021 Jan-Feb;87(1):49-53. doi: 10.4103/ijdvl.IJDVL_588_18.

Abstract

Necrolytic migratory erythema is most commonly associated with glucagonoma syndrome. We report a rare case of glucagonoma syndrome with necrolytic migratory erythema presenting as pruritic papules and follicular pustules in a 57-year-old woman; showing eosinophilic infiltration on histology. However, the final diagnosis was confirmed by demonstrating neuroendocrine tumour on histopathological examination of the liver metastases. Nutrition therapy was administered as a palliative treatment. This case also highlights the atypical clinical features and nonspecific histology of necrolytic migratory erythema which makes the diagnosis difficult.

摘要

坏死松解性游走性红斑最常与胰高血糖素瘤综合征相关。我们报告了一例罕见的胰高血糖素瘤综合征伴坏死松解性游走性红斑的病例,该病例表现为 57 岁女性的瘙痒性丘疹和滤泡脓疱;组织学显示嗜酸性粒细胞浸润。然而,最终诊断通过肝脏转移灶的组织病理学检查显示神经内分泌肿瘤而得到确认。给予营养治疗作为姑息治疗。该病例还突出了坏死松解性游走性红斑的非典型临床特征和非特异性组织学特征,这使得诊断变得困难。

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